NEW APPROACHES IN CANCER PATHOLOGY LESSONS FROM RENAL

NEW APPROACHES IN CANCER PATHOLOGY LESSONS FROM RENAL CARCINOMA STEWART FLEMING UNIVERSITY OF DUNDEE

• MAJOR PARADIGM SHIFT IN EARLY 1990 S IN UNDERSTANDING RENAL CANCER Molecular differential pathology of renal cell tumours G. KOVACS A CLASSIFICATION …BASED ON UNDERSTANDING THE GENETIC ABNORMALITIES INVOLVED WILL BE ROBUST IN TERMS OF BIOLOGY, CLINICAL BEHAVIOUR AND RESPONSE TO THERAPY

GENETIC ALTERATION IN RCC CORRELATES STRONGLY WITH MORPHOLOGY HISTOPATHOLOGY 3 p LOSS VHL MUTATION Y N CLEAR CELL 25 8 18 25 PAPILLARY 1 7 0 8 ONCOCYTOMA 2 3 0 5 CHROMOPHOBE 0 3 FOSTER ET AL 1994 Somatic mutations of the von Hippel - Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma

TUMOUR HISTOLOGY MATTERS BECAUSE IT REVEALS THE UNDERLYING GENETICS WHO v 4 • • • • Clear cell renal cell carcinoma VHL and 3 p– Multilocular clear cell renal cell neoplasm of low malignant potential Papillary renal cell carcinoma c-met and chr 7+; Fumarate hydratase Chromophobe renal cell carcinoma Multiple chromosome loss – Hybrid oncocytic chromophobe tumour Folliculin Carcinoma of the collecting ducts of Bellini Renal medullary carcinoma IN 1 and sickle cell Mi. T family translocation renal cell carcinoma – Xp 11 translocation renal cell carcinoma – t(6; 11) renal cell carcinoma Carcinoma associated with neuroblastoma Mucinous tubular and spindle cell carcinoma Tubulocystic renal cell carcinoma Fumarate hydratase Acquired cystic disease associated renal cell carcinoma Clear cell papillary (tubulopapillary) renal cell carcinoma Hereditary leiomyomatosis associated renal cell carcinoma Fumarate hydratase SDHB associated RCC SDHB Renal cell carcinoma, unclassified

INHERITED RCC • • VHL FAMILIAL PAPILLARY RCC BIRT HOGG DUBE SYNDROME TUBEROUS SCLEROSIS HLRCC SDHB NON-SYNDROMIC FAMILIAL RCC

STAGING Identifies biologically aggressive tumours • The Robson Staging System of Renal Cell Carcinoma – Stage I - Tumour confined within capsule of kidney – Stage II - Tumour invading perinephric fat but still contained within the Gerota fascia – Stage III - Tumour invading the renal vein or inferior vena cava (A), or regional lymph-node involvement (B), or both (C) – Stage IV - Tumour invading adjacent viscera (excluding ipsilateral adrenal) or distant metastases • TNM SYSTEMS ARE A DEVELOPMENT OF THIS CLASSIFICATION • STAGE 1 - 80% 5 y AND 65% 10 y SURVIVAL • WHY DO SOME KIDNEY CONFINED RCCs PROGRESS?

DISSECTION AND SAMPLING MATTER CORRECT DISSECTION OF NEPHRECTOMY SPECIMENS WILL REVEAL EXTRA-RENAL SPREAD Handling and Staging of Renal Cell Carcinoma Kiril Trpkov et al 2013 ISUP Consensus CARDIFF METHOD

MACROSCOPIC EXTENT OF TUMOUR SPREAD • MACROSCOPIC DATA IS REQUIRED FOR ACCURATE TNM 7 STAGING T 3: Tumour extends into major veins or perinephric tissues but not into the ipsilateral adrenal gland not beyond Gerota fascia – T 3 a Tumour grossly extends into the renal vein or its segmental (muscle containing) branches, or tumour invades perirenal and/or renal sinus fat (peripelvic) fat but not beyond Gerota fascia – T 3 b Tumour grossly extends into vena cava below diaphragm – T 3 c Tumour grossly extends into vena cava above the diaphragm or invades the wall of the vena cava

FOUNDER MUTATIONS OFFER AN OPPORTUNITY FOR LIQUID BIOPSY STAGING Plasma genotyping using dd. PCR. Allele specific amplification allows separate identification of wild type and mutant DNA eg VHL mutant DNA Oxnard G R et al. Clin Cancer Res 2014; 20: 1698 -1705

Serial measurement of plasma genotype for disease monitoring. Oxnard G R et al. Clin Cancer Res 2014; 20: 1698 -1705

TUMOUR GRADE PREDICTS BIOLOGY ISUP NUCLEOLAR GRADE • • • Not applicable Grade X - Cannot be assessed Grade 1 - Nucleoli inconspicuous or absent at high power magnification Grade 2 - Nucleoli evident at high power magnification Grade 3 - Nucleoli large and prominent at low power magnification Grade 4 - Nuclei bizarre and/or multilobated, sarcomatoid or rhabdoid morphology • Grade should be assigned according to the worst grade regardless of extent. This system has been validated for clear cell and papillary renal cell carcinoma. It has not been validated for chromophobe and other types of renal cell carcinoma. • HOW DOES IT REFLECT GENETICS?

CHROMOSOMAL CHANGES ARE IMPORTANT PROGNOSTIC MARKERS – PBRM 1 – FHIT – RASSF 1 A – mi. RNA • 9 P LOSS POOR PROGNOSIS EL MOKADEM ET AL 2014 Probability of Cancer Specific Survival % • 3 p LOSS IS MORE THAN LOSS OF wt. VHL Fig 2. Cancer Specific Survival 1 0. 9 0. 8 0. 7 0. 6 0. 5 0. 4 0. 3 0. 2 0. 1 0 0 20 Low 40 60 80 Months Intermediate 100 120 High 140

KINASE PROFILING Pantuck et al 2007

CELL SIGNALLING IS DYNAMIC – IHC STATIC

IHC USEFUL FOR LOCALISING BUT UNRELIABLE FOR QUANTIFYING PHOSPHO-PROTEIN IMMEDIATE 40 MINS GLIOMA XENOGRAFT AKT-P 473 BAKER ET AL CLIN. CANCER RES 2005 MRC PROTEIN PHOSPHORYLATION UNIT USE FRESH TISSUE COLLECTED IN PHOSPHATASE INHIBITORS AND ASSAYED BY BIOCHEMICAL AND WESTERN BLOT METHODS HUANG ET AL BIOCHEM J 2008

CAN WE DEFINE TREATMENT PATHWAYS BY IDENTIFICATION OF DRIVER MUTATIONS? DOES TUMOUR EVOLUTION CONFOUND THAT AIM? SATO ET AL Nat Genet. Aug; 45: 860 -7 (2013)

TUMOUR HETEROGENEITY MORPHOLOGY IMMUNOHISTOCHEMISTRY GRADE • STUDY OF MOLECULAR ALTERATIONS HAS CONFIRMED THAT TUMOUR EVOLUTION IS A BETTER TERM GERLINGER ET AL Nat Genet 46, 225– 233, (2014)

HOW ARE WE TO IDENTIFY DRIVER MUTATIONS TO PLAN TREATMENT? Ricketts& Linehan Nature Genetics (2014) GUIDED SAMPLING AND THE ROLE OF THE PATHOLOGIST

LEARNING FROM FAILURE

Overall survival curves of patients with a KRAS-mutated and nonmutated tumor. Responders 0/13 had Ki. Ras mutation Non-responders 13/19 has Ki. Ras mutation Lièvre A et al. Cancer Res 2006; 66: 3992 -3995 WHAT IS THE BIOLOGY OF TREATMENT FAILURE IN RCC?

MOLECULAR PATHOLOGY • Protocols for molecular genetic techniques need to standardized, thresholds agreed upon, sampling of tissues needs to be assessed and interobserver agreement reported. • The results of new and emerging molecular genetic techniques need to be validated including appropriate use of negative and positive controls.

RENAL CELL CARCINOMA WHAT REALLY MATTERS? genetics